Align 4-hydroxybutyrate-CoA ligase (EC 6.2.1.40) (characterized)
to candidate WP_068112231.1 I601_RS16760 fatty acid--CoA ligase
Query= BRENDA::A4YDR9 (549 letters) >NCBI__GCF_001653335.1:WP_068112231.1 Length = 550 Score = 206 bits (525), Expect = 1e-57 Identities = 152/511 (29%), Positives = 249/511 (48%), Gaps = 34/511 (6%) Query: 49 TYSTFYDNVMVQASALMRRGFSREDKLSFISRNRPEFLESFFGVPYAGGVLVPINFRLSP 108 +YS + A+AL G + ++ N E LE++ VP G VL +N RL P Sbjct: 40 SYSELGERTARLANALRGLGVDGDQRVGTFQWNNVEHLEAYLAVPSMGAVLHTLNIRLFP 99 Query: 109 KEMAYIINHSDSKFVVVDEPYLNSLLEVKDQIKA-EIILLEDPDNPSASETAR----KEV 163 +++ Y+ NH+ V+VD+ + L Q+ E +++ PD+ A A K+V Sbjct: 100 EQLVYVANHAQDHVVIVDDSLVGLLAPHLGQMTTVEHVVVAGPDSADADLDALRATGKQV 159 Query: 164 RMTYRELVKGGSRDPLPI--PAKEEYSMITLYYTSGTTGLPKGVMHHHRGAFLNAMAEVL 221 + Y +L+ + P P +E + YTSGTTG PKGV++ HR A+L+++A Sbjct: 160 HL-YEDLL---AMQPTTFDWPELDERDAAAMCYTSGTTGNPKGVVYSHRSAYLHSLAVCG 215 Query: 222 EHQMDLN--SVYLWTLPMFHAASWGFSWATVAVGATNVCLDK-VDYPLIYRLVEKERVTH 278 + L+ L +PMFHA +WG ++ + GA+ D+ + + R +++ R T Sbjct: 216 GNTTALSFEDRVLPIVPMFHANAWGLPYSAMMSGASLCLPDRWLQADPLVRFIQESRPTL 275 Query: 279 MCAAPTVYVNLADYMKRNNLKFSNRVHMLVAGAAPAPATLK-AMQEIGGYMCH-VYGLTE 336 PTV+ ++ ++ + + + +++ G + P +L+ A+QE G + +G+TE Sbjct: 276 SGGVPTVWNDVLSHLDAHPEVALDSLRLVLCGGSAVPVSLQQALQERHGLLVRQAWGMTE 335 Query: 337 TYGPHSICEWRREWDSLPL-----EEQAKLKARQGIPYVSFEMDVFDANGKPVPWDGKTI 391 T S LP EEQ + + QG + + +P DG+++ Sbjct: 336 TSPVASA--------GLPPVGCSEEEQWQYRGTQGRLLCGVSARIVADDQTVLPHDGRSV 387 Query: 392 GEVVMRGHNVALGYYKNPE----KTAESFRDGWFHSGDAAVVHPDGYIEIVDRFKDLINT 447 GE+ +RG V YY+ E + F DGW +GD V GYI + DR KD+I + Sbjct: 388 GELEVRGPWVTAAYYRPEEGERAEAEAKFHDGWLRTGDVGHVDELGYISLTDRAKDVIKS 447 Query: 448 GGEKVSSILVEKTLMEIPGVKAVAVYGTPDEKWGEVVTARIELQEGVKLTEEEVIKFCKE 507 GGE +SS+ +E LM V AV PDEKW E A + +++G +T EE+ +F Sbjct: 448 GGEWISSVDLENALMAHEAVLEAAVVAIPDEKWQERPLASVVVRDGATVTVEELREFLSR 507 Query: 508 RLAHFECPKIVEF-GPIPMTATGKMQKYVLR 537 A ++ P F +P T+ GK K VLR Sbjct: 508 DFAKWQLPDTWAFIDEVPRTSVGKFDKKVLR 538 Lambda K H 0.319 0.136 0.411 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 707 Number of extensions: 32 Number of successful extensions: 6 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 549 Length of database: 550 Length adjustment: 36 Effective length of query: 513 Effective length of database: 514 Effective search space: 263682 Effective search space used: 263682 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 53 (25.0 bits)
This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory